Scientific Reports (Jan 2023)

Impact of plasmapheresis on severe COVID-19

  • G. Fonseca-González,
  • M. Alamilla-Sánchez,
  • V. García-Macas,
  • J. Herrera-Acevedo,
  • M. Villalobos-Brito,
  • E. Tapia-Rangel,
  • D. Maldonado-Tapia,
  • M. López-Mendoza,
  • J. H. Cano-Cervantes,
  • J. Orozco-Vázquez,
  • D. Timarán-Montenegro,
  • S. Cortés-Martínez,
  • M. Escarela-Serrano,
  • S. Muñoz-López,
  • L. Montiel-López,
  • P. Mondragón-Terán,
  • J. A. Suárez-Cuenca

DOI
https://doi.org/10.1038/s41598-022-25930-8
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 8

Abstract

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Abstract The clinical course of COVID-19 may show severe presentation, potentially involving dynamic cytokine storms and T cell lymphopenia, which are leading causes of death in patients with SARS-CoV-2 infection. Plasma exchange therapy (PLEX) effectively removes pro-inflammatory factors, modulating and restoring innate and adaptive immune responses. This clinical trial aimed to evaluate the impact of PLEX on the survival of patients with severe SARS-CoV-2 and the effect on the cytokine release syndrome. Hospitalized patients diagnosed with SARS-CoV-2 infection and cytokine storm syndrome were selected to receive 2 sessions of PLEX or standard therapy. Primary outcome was all-cause 60-days mortality; secondary outcome was requirement of mechanical ventilation, SOFA, NEWs-2 scores modification, reduction of pro-inflammatory biomarkers and hospitalization time. Twenty patients received PLEX were compared against 40 patients receiving standard therapy. PLEX reduced 60-days mortality (50% vs 20%; OR 0.25, 95%CI 0.071–0.880; p = 0.029), and this effect was independent from demographic variables and drug therapies used. PLEX significantly decreased SOFA, NEWs-2, pro-inflammatory mediators and increased lymphocyte count, accompanied with a trend to reduce affected lung volume, without effect on SatO2/FiO2 indicator or mechanical ventilation requirement. PLEX therapy provided significant benefits of pro-inflammatory clearance and reduction of 60-days mortality in selected patients with COVID-19, without significant adverse events.